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Article

Relative Safety of Sexual Lubricants for Rectal Intercourse

SUDOL, KRISTIN M. BA; PHILLIPS, DAVID M. PhD

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Sexually Transmitted Diseases: June 2004 - Volume 31 - Issue 6 - p 346-349
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THE LARGE MAJORITY OF men who have sex with men (MSM) use lubricants during rectal sex. 1 Several years ago, a large survey of MSM found that 42% of the men reported that they chose lubricants containing N-9. 1 However, we have demonstrated that rectal application of N-9 in mice enhances the probability that an animal will become infected after rectal challenge with Herpes simplex virus (HSV-2). 2 Furthermore, studies have demonstrated that N-9 causes rapid sloughing of the rectal epithelium in animals and humans. 2–4 These observations lead a number of organizations, including the Centers for Disease Control and Prevention (CDC), 5 the World Health Organization (WHO), and CONRAD, 6 to recommend that N-9 products should not be used rectally.

These findings raise the question of which sexual lubricants are safest for rectal use. Many sexual lubricants contain high concentrations of cytotoxic preservatives and/or excipients that could possibly result in damage to the rectal epithelium (similar to that caused by N-9).

This report describes a direct and nonlabor-intensive mouse model that can be used to determine the degree to which a lubricant causes sloughing of the rectal epithelium. In addition, a standard cytotoxicity assay has been used. Enhancement of HSV-2 infection after rectal challenge was used to assay the degree to which lubricants enhance infection. Using these methodologies, several lubricants could be compared in terms of rectal safety.

Materials and Methods

Test Formulations

Test formulations were water-based Vagisil (Combe Inc., White Plains, NY), Astroglide (Biofilm Inc., Vista, CA), Viamor (Women First HealthCare Inc., San Diego, CA), and Delube (E-Gal Corp., Highland Park, IL), carrageenan-based Carraguard—an investigational new drug of the Population Council 7 —and a methylcellulose formulation. 7 KY-Plus (containing nonoxynol-9; Advanced Care Products, Raritan, NJ) was used as a positive control and phosphate-buffered saline (PBS) (Gidco, Grand Island, NY) served as a negative control.

Animals

Six- to 8-week-old female BALB/c mice (Charles River, Wilmington, MA) were maintained on a 12-hour light cycle at the Rockefeller University Laboratory Animal Research Center according to university guidelines. Animals were group housed, and food and water was available ad libitum.

Propagating Virus

Methods for propagating and titering HSV-2 have been previously described. 8

MTT Cytotoxicity Assay

Cytotoxicity of serial dilutions of compound was assayed using the MTT (thiazolyl blue) colorimetric assay, in which color saturation (absorbance) is directly proportional to cell density. Propagation of ME-180 epithelial cells has been previously described with the following changes. 9 Fifty microliters of RPMI (Invitrogen, Carlsbad, CA) containing various concentrations of the test compound dilutions were added to a Falcon 96-well assay plate (Becton Dickinson, Franklin Lakes, NJ) containing confluent epithelial-like human cervical (ME-180) cells. Plates were incubated for 2 hours at 37°C and 5% CO2. Wells were subsequently washed 3 times with 100 μL of RPMI. Twenty microliters of MTT reagent (Promega, Madison, WI) was added to each well. After a 1-hour incubation period at room temperature, absorbance was read on a plate reader at 490 nm.

Rectal HSV-2 Challenge

Food was withheld for 24 hours. Subsequently, 0.1 mL of a solution of 1 mL of dissolved Ketamine (Fort Dodge Laboratories, Fort Dodge, IA) with 0.5 mL of xylazine (Miles Inc., Shawnee Mission, KS) in 6.75 mL PBS was injected intraperitoneally (IP) to immobilize the animals and prevent defecation. Once anesthetized, mice were rectally treated with 20 μL of test formulations using a positive placement Gilson Microman pipette. Five minutes later, mice were challenged rectally with 10 μL of DMEM (Dulbecco’s Modified Eagle Medium; Gibco, Bethesda, MD) containing 5 × 104 plaque-forming units (PFU; 50% infection dose) of HSV-2 using a M20 Pipetman. A 14-day observation period followed rectal challenge. Animals displaying redness, swelling, hair loss, and/or lesions in the rectal area were scored as positive and euthanized.

Rectal Sloughing

It has been previously observed that N-9 causes rectal sloughing in mice, monkeys, and humans. 2–4 Based on this observation, an assay to quantify the number of epithelial cells in the rectum following product insertion was developed. To carry out these studies, food was withheld and animals were anesthetized as described previously. Once anesthetized, 20 μL of test formulation was placed in the mouse rectum using a Microman. Fifteen minutes later, the rectum was lavaged 5 times with 20 μL PBS. The 5 lavages were pooled, and 10 μL trypsin-EDTA was added. Subsequently, the washes were incubated at 37°C and 5% CO2 for 15 minutes. This procedure was carried out to separate individual epithelial cells from each other. After incubation, 10 μL of fetal bovine serum (Invitrogen, Carlsbad, CA) was added to inhibit trypsin. Cells were counted in a Coulter Z2 Particle Count (Coulter Corp., Miami, FL). Each sample was counted 3 times. The averages from each sample reading were calculated, and the standard deviation was determined.

Results are expressed as mean ± standard deviation (SD). Data were subjected to analysis of variance for group analysis of variance. A P value ≤0.05 was considered significant.

Results

MTT Cytotoxicity Assay

The degree of cytotoxic effect varied widely. Carraguard and methylcellulose were not cytotoxic, even when diluted 1:1 with medium. KY-Plus was 50% cytotoxic as compared with control (no formulation) when diluted 330 times (Fig. 1;Table 1).

TABLE 1
TABLE 1:
Comparison of Cytotoxicity of Different Products
Fig. 1
Fig. 1:
Results of cytotoxicity assay. Serial dilutions of all formulations were tested using the MTT assay with ME-180 epithelial cells. This figure presents data for Carraguard and Astroglide. Carraguard is not cytotoxic used at a concentration of 20% (diluted 1:5 in cell culture medium), whereas Astroglide is 50% cytotoxic at a concentration of approximately 2.5% (diluted 1:32 in cell culture medium).

Rectal HSV-2

Infection Assay Because we wanted to determine protection from or enhancement of infection, we chose a dose of HSV-2 known to infect 50% of the mice. Carraguard showed significant protection from infection (P <0.05) as compared with PBS. Delube and KY-Plus significantly increased infection as compared with PBS (P <0.01) (Fig. 2;Table 2).

TABLE 2
TABLE 2:
Summary of the 3 Assays Used to Access Topical Rectal Cytotoxicity*
Fig. 2
Fig. 2:
Protection after rectal challenge with a 50% infectious dose of HSV-2. Viamor, Vagisil, and Astroglide had a tendency to enhance infection, but it was not significant. Pretreatment with Delube or KY Plus resulted in a significant increase in the number of infected mice. Error bars represent the standard deviation of 3 readings per mouse for each of 10 mice per compound.

Rectal Sloughing Assay

The average number of cells that were sloughed varied widely among products. The number of cells recovered after treatment of methylcellulose and Carraguard formulations was similar (approximately 2 × 106/mL). In sharp contrast, more than 10 times the number of cells (approximately 6 × 107/mL) was recovered from mice that were treated rectally with Viamor, Vagisil, or Astroglide. All were highly significant (P <0.01) compared with PBS. At least another order of magnitude of cells (approximately 8 × 108/mL) was recovered from the rectums of mice pretreated with Delube or KY-plus (Fig. 3). This difference was highly significant compared with Viamor, Vagisil, or Astroglide (P <0.01).

Fig. 3
Fig. 3:
Number of cells recovered from the rectum of mice 15 minutes after rectal application of the product. There are more than 2 orders of magnitude of difference between products. Methylcellulose, phosphate-buffered saline, and Carraguard were not significantly different from each other (P = 0.139). Vagisil differed significantly from Carraguard (P <0.01), and the differences between Viamor and Vagisil, Astroglide and Viamor, Delube and Astroglide, and KY Plus and Delube were all significant (P <0.01). Error bars represent the standard deviation of 3 readings per mouse for each of 10 mice per compound.

Discussion

Three different assays were used to determine the relative deleterious effect on the rectal epithelium of several sexual lubricants. The findings are summarized in Table 2. As shown by our assays, 1 of these products, Delube, which contains benzalkonium chloride, is just as cytotoxic for rectal use as KY-Plus, a 2.2% N-9 product. The other sexual lubricants tested, Astroglide, Vagisil, and Viamor, are far less cytotoxic than Delube, but they still have significant rectal cytotoxicity. The only products that do not exhibit any cytotoxicity are Carraguard and methylcellulose, which are not yet commercially available. We plan to use the assays described here to test more commercially available sexual lubricants in the hope of identifying those that appear to be safe for rectal use.

Recently, Baron et al. 10 assayed several sexual lubricants for activity against HIV in vitro. They found that some sexual lubricants, including Astroglide, Vagisil, Viamor, and N-9, blocked HIV infection of lymphoma cells. The authors suggested that these products should be explored as possible HIV preventatives. We caution that any anti-HIV properties are most likely related to general cytotoxicity. The formulations with the greatest anti-HIV activity are likely to breach the delicate epithelia of the rectum and lower intestinal tract. Thus, although they could have some anti-HIV activity, these products should not be used as rectal lubricants.

Preservatives and/or excipients contained in the lubricants could be the agents responsible for rectal cytotoxicity. In this regard, both Carraguard and the methylcellulose formulation have sufficient concentrations of preservatives to pass the preservative effectiveness tests required by the U.S. Food and Drug Administration for vaginal products, and they contain no other excipients. Thus, we speculate that the concentration or type of preservatives and/or excipients in some sexual lubricants could be excessive.

We have developed a sensitive quantitative assay to measure cell sloughing of the rectal epithelium. Although this assay measures rectal epithelial sloughing in mice only, human rectal studies have been found to correlate strongly to murine rectal studies. 3 Other current animal systems that access topical cytotoxicity are problematic. The rabbit eye model is not sensitive enough to distinguish among products with relatively minor differences in topical cytotoxicity. 11 Similarly, in the rabbit dermal irritation study, minor differences in irritability are difficult to detect. 11 Although the rabbit vaginal irritation model is quantitative, it is somewhat subjective because it relies on relative scores from examination of histology. 11,12 In addition, these assays are costly, because rabbits are relatively expensive animals. The system described here is quantitative, is not very time-consuming (cells are counted in a Coulter counter), and is inexpensive because mice are relatively inexpensive. Thus, the cell sloughing assay described here could be useful for assaying topical cytotoxicity of formulations under development for a variety of topical applications.

Lastly, we emphasize that this study deals exclusively with rectal safety. The rectal epithelium is an absorptive tissue with a delicate simple columnar epithelium. In sharp contrast, the human vagina is lined by a multilayered stratified squamous epithelium designed for the strain that can occur during sexual intercourse and childbirth. Thus, products that could be hazardous for rectal use could be safe for vaginal use. For instance, vaginal spermicides containing N-9 are of particular importance because, in many cases, they are the only contraceptives readily available to certain populations of women. No conclusions can be drawn about vaginal safety of sexual lubricants from this article.

References

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